25616-33-5
Chemical Structure
Boc-Phe-Gly-OH
- CAS No.: 25616-33-5
- Formula:C16H22N2O5
- Molecular Weight:322.36
IUPAC Name: (tert-butoxycarbonyl)-L-phenylalanylglycine
InChIKey: MJRWXIQFTMLYFG-LBPRGKRZSA-N
SMILES: O=C(O)CNC([C@H](CC1=CC=CC=C1)NC(OC(C)(C)C)=O)=O
Biological Activity: Boc-Phe-Gly-OH is an N-Boc protected dipeptide, consisting of N-tert-butoxycarbonyl (Boc)-protected phenylalanine and glycine. Boc-Phe-Gly-OH serves as an intermediate in organic synthesis-related research[1][2].
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Boc-Phe-Gly-OH | 99.44% | Boc-Phe-Gly-OH is an N-Boc protected dipeptide, consisting of N-tert-butoxycarbonyl (Boc)-protected phenylalanine and glycine. Boc-Phe-Gly-OH serves as an intermediate in organic synthesis-related research. | ||||||||||||||||||||
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References
- [1]. Liu Z, et al. N-Boc deprotection and isolation method for water-soluble zwitterionic compounds. The Journal of organic chemistry. 2014 Dec 05;79(23):11792-6.
- [2]. Das P, et al. Single-stranded DNA detection by solvent-induced assemblies of a metallo-peptide-based complex. Nanoscale. 2016 May 05;8(18):9527-36.